Medline recalls Centurion procedure packs with Caina syringes (MNS11965A, CIT6720, CIT6720A) due to leaks and breakage risks that could harm patients.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
Medline is recalling Centurion procedure packs containing Caina syringes because leaks and breakage may pose health risks to patients. This affects medical kits used for procedures like arthrograms and circumcisions.
The syringes in these packs can leak or break, potentially causing patient health issues. This is linked to a FDA safety alert from March 19, 2024, which identified quality problems with the syringes.
Healthcare providers using these procedure packs for medical procedures are most at risk. Patients receiving care with these kits could be affected if the syringes leak or break.
Check for packs labeled 'ARTHROGRAM TRAY' (Pack Number MNS11965A) or 'CIRCUMCISION TRAY' (Pack Numbers CIT6720 or CIT6720A). The lot numbers are 2023040690, 2022122390, and 2023110890 respectively.
Look for specific pack numbers and lot numbers listed in the recall notice to confirm if your kit is affected.
The syringes can leak or break, which may pose a risk to patient health as noted in the FDA safety alert from March 19, 2024.
These packs are used for procedures like arthrograms and circumcisions.
Check for the specific pack numbers and lot numbers: MNS11965A (Lot 2023040690), CIT6720 (Lot 2022122390), or CIT6720A (Lot 2023110890).
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-2779-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-2779-2024 from Medline Industries. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
